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FDA 510(k) Applications Submitted by JASON BLAIN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040276
02/05/2004
QUANTUM CEMENT RESTRICTOR
QUANTUM ORTHOPEDICS
K050449
02/22/2005
QUANTUM VERTEBRAL BODY REPLACEMENT
QUANTUM ORTHOPEDICS, INC.
K060491
02/24/2006
QUANTUM ANTERIOR CERVICAL PLATE SYSTEM
QUANTUM ORTHOPEDICS, INC.
K141372
05/27/2014
MERCURY SPINAL SYSTEM
SPINAL ELEMENTS, INC.
K991882
06/02/1999
NEXFLEX TOTAL KNEE SYSTEM
NEXMED, INC.
K061576
06/07/2006
MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT SYSTEM
QUANTUM ORTHOPEDICS, INC.
K992350
07/14/1999
PYLON INTRAMEDULLAARY NAIL SYSTEM
ALPHATEC MFG., INC.
K052641
09/26/2005
MODIFICATION TO: QUANTUM VERTEBRAL BODY REPLACEMENT
QUANTUM ORTHOPEDICS, INC.
K993513
10/18/1999
DELTALOC ANTERIOR CERVICAL PLATE SYSTEM
ALPHATEC MFG., INC.
K993873
11/15/1999
ALPHATEC EXTERNAL FIXATION SYSTEM COMPRESSION/DISTRACTION ROD
ALPHATEC MFG., INC.
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